|
Energetic and Enthusiastic Field Based CRA I – UK and EU sites |
| Posted: |
16/05/08 |
 |
| Recruiter: | 1st-itpeople.com |
| Reference: | LYD - 91 |
| Type: | Contract |
| Language: | English, Polish |
| Salary: | EUR30000 - EUR35000 per annum + laptop, travel costs and phone |
| Benefits: | |
| Location: | Poland |
| Description: |
Energetic and Enthusiastic Field Based CRA I – UK and EU sites
Contact Information:
Lee Dunn
Tel: +44 (0) 207 255 6665
Lee.dunn@1st-pharmapeople.com
http://www.1st-pharmapeople.com
Job Summary:
This is a home based clinical research associate role from any EU country, monitoring sites already set-up and projects pipelined across the UK and EU (Germany, Spain, Italy, France, Belgium, Poland etc). The role is a fixed term contract, for a 24 Month project with very high chance to be permanent after to facilitate promotions. There is training involved as well as Co-monitoring opportunities in the USA. Additional EU language skills are VERY desirable.
Offers:
This role offers: Home based working, monitoring international trials within a global CRO. Lose supervision and access to European sites and projects based on additional language skills. There is training and co-monitoring opportunities within the USA as well as excellent promotional opportunities within. The work ethic is very forward thinking and there is a very family orientated feel to the company.
There is a fixed term salary of £29,000.00/€36,000.00, no extra benefits. Laptop, training, phone line cover, travel expenses are all picked up by the company.
Candidates:
Need a Life Sciences Degree, Nursing or international equivalent. A second European language is very desirable but not essential as is EU monitoring experience.
6 to12 Months monitoring experience in any European country (Spain, Italy, Poland, Belgium, UK etc)
Personal flexibility to travel within the EU for monitoring (60%) and to the USA for sites and training. Personality is key within this company and we candidates must be enthusiastic, willing to learn, travel and gain promotions. Management is loose but very hands-on and supportive.
Experience with Ethics and Regulatory Affairs will be very well received.
Responsibility Brief:
Your main duties will be to monitor allocated sites to ensure that the monitoring process complies with relevant SOPs, GCP and regulatory requirements.
Contribute to the in-house review of Case Report Form and to perform queries resolution.
Report and follow up on Serious Adverse Events
You will also have to conduct site initiations, start-up and closeout monitoring visits along with preparation and delivery of presentations at investigators meetings.
Manage trip reports, letters, query resolutions and expenses.
Maintain regular communication with the sites, report in writing all sites visits and other contacts, ensuring that the Clinical Project Manager is informed of the study progress and/or any problems with the sites
Supporting the preparation of Clinical Study Reports, annual IND Safety Reports, and clinical sections
If you would to discuss this role in greater detail or your application / suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.
This company is acting as an Agency and/or Employment Business
Clinical Research, CRA, Clinical Research Associate, Study Manager, Study Management, Project Manager, Clinical Study, Clinical Studies, Clinical Trial, Clinical Trials and Clinical Development, Phase I, Research Physician, Medical Doctor, ICH GCP, Good Clinical Practice, GCP and Drug Development
1st IT People Limited is acting as an Employment Agency and/or Employment Business |
|
|
|    |
